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1 g the acid-catalyzed degradation reaction of erythromycin A.
2 was not detected in controls with or without erythromycin A.
3 acid stability of erythromycin B relative to erythromycin A.
5 cursor-directed biosynthesis of 15-propargyl erythromycin A, a novel antibiotic that not only is as p
6 ae, as well as improved activity compared to erythromycin A against the inducibly MLS (macrolide, lin
7 -dihydro-9-acetamido-N-desmethyl-N-isopropyl erythromycin A analogues and related derivatives was gen
11 ndustrial-scale production of the antibiotic erythromycin A, derivatives of which play a vital role i
13 e is much more stable than the corresponding erythromycin A ester, degrading nearly 40 times more slo
16 Three polyketide natural products, namely erythromycin A, lasalocid A, and iso-lasalocid A, were s
17 l drugs--norfloxacin, a fluoroquinolone, and erythromycin, a macrolide--proteins with single mutation
19 epithelial cells, effects of doxycycline and erythromycin A on inducible NO synthase (iNOS) NO produc
22 any link between this and the modulation of erythromycin A titre, which has been observed for S. ery
24 e the extent of CYP3A-mediated metabolism of erythromycin, a widely used model substrate for CYP3A.
25 vel antibiotic that not only is as potent as erythromycin A with respect to its ability to inhibit ba
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